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ASD - Quality Assurance Specialist II
Ref No.: 18-13689
Location: Pomona, California
Role: Quality Assurance Specialist II
Location: Pomona, CA
Duration: 5+ Months Contract

Responsibilities:

Reviewing raw data for technical reports
Writing Design Validation/Process Validation protocols and final reports.
Creating batch records and other Design Master Record (DMR) documents
Revising SOPs and other documents

Qualifications:
BS Degree, Chemistry, Biochemistry, Microbiology and Biology preferred
3-5 years In-Vitro Diagnostics (IVD) medical Device, Pharmaceutical or Medical Device experience
Design Verification and/or Design Validation/Process Validation experience helpful
Experience with QA and/or R&D technical documentation (Agile experience preferred)
Quality focused, detail oriented, able to learn quickly